HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376974Generated: October 30, 2026
Ethyl Thioglycolate → HCID 53677012, compound
https://huagongshe.com/reaction/376974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 18755078 | HCID 18755078 | — |
| Product | HCID 53677012 | HCID 53677012 | — |
Reaction Steps
5.9 g (19.1 mmol) of 1-[4-(2-hydroxyethylthio)-phenyl]-2-methyl-2-morpholin-4-yl-propan-1-one, 4.2 ml (38.2 mmol) of ethyl thioglycolate, and 4.4 g (22.9 mmol) of p-toluenesulfonic acid monohydrate are mixed and stirred at 100° C. for 24 h. Then the solution is cooled to room temperature and neutralized with 1N NaOH. The crude product is extracted with ethyl acetate, washed with saturated sodium chloride solution, dried over MgSO4, and concentrated. The residue is purified by column chromatography on silica gel with ethyl acetate -hexane (30:70) as an eluent. The structure is confirmed by the 1H-NMR spectrum (CDCl3): δ [ppm] 1.31 (s, 6H), 1.99 (t, 1H), 2.57 (t, 4H), 3.22-3.30 (m, 4H), 3.70 (t, 4H), 4.36 (t, 2H), 7.34 (d, 2H), 8.51 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06022906 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-50924bbc24e049a9bf71de8de0ecbc5f |
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| Source note | uspto-grants-2000_02 |
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